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Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b).

Idiopathic Pulmonary Fibrosis (IPF) as the name suggests is a progressive disorder with no known aetiology. It is characterised by the thickening of the alveoli due to scarring resulting in cough. It is known to primarily occur in older adults over 60 years of age. The findings of IPF have a known association of Usual Interstitial Pneumonia (UIP) (Raghu et al., 2011; Kawano-Dourado & Kairalla, 2013; Wells, 2013). It has been deemed that the prognosis is generally poor when UIP has been confirmed (King et al., 2001b). The median survival rate of IPF is 50%, typically around two years after diagnosis (Raghu et al., 2011; King et al., 2001b).

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smoking (Rosas et al., 2007; Steele et al., 2005). The samples of lung biopsy from individual<br />

with early asymptomatic lung disease exhibit several histologic subtypes of interstitial lung<br />

disease (ILD) (Rosas et al., 2007). A familiar risk factor for few idiopathic interstitial<br />

pneumonias including IPF is cigarette smoking (Baumgartner et al., 1997), it may result in<br />

subclinical parenchymal lung disease that is observable by spirometry and computed<br />

tomography (CT) imaging, even amidst a conventionally healthy cohort (Lederer et al., 2009;<br />

Washko et al., 2010). A high-resolution CT (HRCT) scanning emerges to be more sensitive<br />

than measurements of pulmonary function and cardiopulmonary exercise test parameters in<br />

recognizing subjects with asymptomatic ILD (Rosas et al., 2007).<br />

It is uncertain presently that how patients with incidental, subclinical IPF should be<br />

attended and supervised. It is significant to have enhanced comprehension since the<br />

prevalence of subclinical IPF is probable to expand with expanding tendency in the operation<br />

of chest CT imaging for non-ILD diseases, like the diagnosis of pulmonary embolism and<br />

coronary artery disease. Considering the comparable low prevalence of IPF and deficiency of<br />

successful therapies, it is also unknown how to recognize those at high risk for progressing<br />

IPF in the general population and if the screening attempts to modify the results perceive in<br />

the subclinical stage IPF. It is probable additionally that subclinical IPF is not a benign<br />

procedure. The subclinical IPF may be exhibited as a risk factor for the progression of acute<br />

aggravation, basically after invasive process or (Chida et al., 2008; Araya et al., 2008;<br />

Takeda et al., 2008) .<br />

2.2.7.2 Slowly Progressive IPF<br />

In the IPF’s traditional phenotype there is gradually continuous decrease in the lung<br />

function and aggravating dyspnea causing death within some years of diagnosis (Selman et<br />

al., 2007; King et al., 2001b). In aggravating disease the mean annual rate of decrease, ranges<br />

from 0.13 L to 0.21 L as measured by the FVC (King et al., 2008; Raghu et al., 2004; Azuma<br />

et al., 2005; Demedts et al., 2001; Taniguchi et al., 2010; Raghu et al., 2008; Daniels et al.,<br />

2010). It is observed that the gradually continuous clinical path may basically be less usual<br />

than classically defined. According to a current population-based cohort study in Olmsted<br />

County, Minnesota, 47 incident cases of IPF were evaluated over a term of 9-years and<br />

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